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Rehabilitation of Patients With Modic Changes in the Lumbar Spine

Rehabilitation of Patients With Modic Changes in the Lumbar Spine - a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00454792
Enrollment
100
Registered
2007-04-02
Start date
2007-03-31
Completion date
2011-09-30
Last updated
2011-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain

Keywords

Low back pain, Modic changes

Brief summary

The purpose of this study is to compare patients with low back pain (LBP) and Modic Changes from The Backcenter Funen, Ringe: 1. To compare the effect of two types of non-operative treatments: A. exercise and advice to be physically active B. restitution and advice not to overload the spine 2. To investigate if the results of the treatment are influenced by gender, age, smoking, and physical load.

Detailed description

The clinical experience is that many patients with Modic changes have relatively severe and persistent LBP, which typically appears to be resistant to treatment. Furthermore, a retrospective study at The Backcenter Funen, Ringe, shows that patients with MC fail to improve engaging physical activity. This is unfortunate, because the typical rehabilitation for patients with persistent LBP is back exercises and information about keeping physically active. This means that this relatively large subgroup of patients with Modic changes probably does not improve with the rehabilitation tools used today. A randomised controlled trial has therefore been designed to study the specific subgroup of patients with Modic changes. In this study we will compare the present state-of-the art rehabilitation approach to persistent LBP (namely to exercise and keep active) with a new concept (restitution). The justification for this is that restitution reduces mechanical stress on the vertebrae and therefore would allow heeling of the possible micro fractures in Modic changes.

Interventions

OTHERExercise

Back exercise: At home every day. In groups once a week. Duration 10 weeks.

OTHERRestitution

Restitution: At home 2 times one hour. Meetings every 2 weeks. Duration 10 weeks.

Sponsors

Velux Fonden
CollaboratorOTHER
The Back Research Center, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Primary inclusion criteria for receiving MRI * The patient must have LBP with a current duration of 3 - 12 month. * The patient must have an actual pain intensity ≥4 on numerical pain rating scale from 0-10. Secondary inclusion criteria for receiving MRI * The patient must speak and understand Danish. * The patient must be between 18-60 years of age. * The patient must be willing to participate in the project. Inclusions criterium for the project * There must be an MRI showing MC in the lumbar spine.

Exclusion criteria

* The patient is unable to go through with the project because of other physical or mental disorder. * The patient is pregnant. * The patient is referred to operation.

Design outcomes

Primary

MeasureTime frame
The primary outcome measure is actual LBP, as measured with an 11 point box scale.10 weeks and 12 months

Secondary

MeasureTime frame
General Health, as measured with the EQ-5D (EuroQol)10 weeks and 12 months
General improvement, as measured with two global instruments a 7-point transition question and an assessment score consisting of a bothersomeness index10 weeks and 12 months
Physical functions measured with Roland Morris Disability Questionnaire10 weeks and 12 months

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026